Vaccines containing modified allergenic material

ABSTRACT

Pharmaceutical preparations for parenteral administration are provided from modified allergenic material and a parenterally acceptable carrier. An adjuvant such as tyrosine may be included.

United States Patent 1 [111 3,761,585

Mullan et al. Sept. 25, 1973 VACCINES CONTAINING MODIFIED [52] US. Cl. 424/91, 260/112 ALLERGENIC MATERIAL [51] Int. Cl Afilk 27/ 14 [75] Inventors: Noel Austin Mullan; Brian [58] Field of Search 424/91 Overell, both of Dorking, England Primary Examiner--Richard L. Huff AttorneyJacobs & Jacobs [73] Assignee: Beecham Group Limited,

Middlesex, England [57] ABSTRACT Pharmaceutical preparations for parenteral administra- [22] Filed 1971 tion are provided from modified allergenic material [21] App]. No.: 131,500 and a parenterally acceptable carrier. An adjuvant such Related US. Application Data as tyrosme may be Included [62] Division of Ser. No. 59,745, July 30, 1970. 16 Claims, N0 Drawings VACCINES CONTAINING MODIFIED ALLERGENIC MATERIAL This application is a division of our copending application Ser. No. 59,745 filed July 30, 1970.

The present invention relates to desensitizing or immunizing agents useful in the treatment of hypersensitive or allergic conditions, and to a method for their preparation.

It is well known that some individuals are allergic or hypersensitive to certain allergenic materials such as pollens, house dust, cat fur, cereals and a host of other common substances. Such individuals can suffer acute discomfort as a result of their allergic conditions which may manifest themselves in such diseases as asthma, hay fever, eczema, dermatitis and migraine. Consequently work continues to find suitable treatments which will alleviate the suffering of the allergic patient.

One technique which has been used in the past in the treatment of allergic conditions is the so-called desensitization therapy. The patient undergoing such therapy is administered repeated gradually increasing doses of an extract of the particular allergenic material or materials to which he is sensitive. At the end of a course of treatment the patients natural resistance to the allergen is usually greatly enhanced, presumably as a result of the build-up of antibodies in his body, stimulated by the administered extract.

As will be appreciated, this desensitization therapy suffers from certain disadvantages, not the least of which lies in the possibilities that a dangerously high dose of allergen may inadvertently be administered, resulting in a general anaphylactic reaction in the patient. It has been suggested that this problem would be overcome if it were possible to modify the allergenic material in such a way that their immunizing is reduced relative to their desensitizing and/or immunising properties. In other words, if the allergenic material could be rendered harmless, or at least less harmful to the sensitive patient, while at the time retaining its ability to stimulate antibody production, one of the main disadvantages of desensitization therapy could be removed.

According to the present invention there is provided a process for the preparation of a modified allergenic material, which process comprises the reaction of an allergenic material with a polyaldehyde, a polyketone, a carbodiimide, an epihalohydrin or an inorganic cyanate, with the proviso that when an inorganic cyanate is employed the reaction is carried out under acid conditions.

The allergenic starting material which is modified according to the process of this invention may be obtained from an allergen-containing substance such as pollen by extracting the allergen-containing substance with a suitable solvent, usually aqueous, in a known manner. The allergenic extract obtained in this way consists principally of protein or glycoprotein, usually contaminated with free carbohydrate. The allergenic extract is then usually purified by removing some of the contaminants, e.g. by dialysis, precipitation or gel filtration, and the resulting purified allergenic material may then be treated according to the process of invention. A fuller description of some of the techniques available can be found in an article by J.N.Newell in the Journal of Allergy, Vol. 13, 1942, pages 177 to 203, particularly page 187. In another useful extraction procedure, the allergen-containing material or an aqueous extract thereof is treated with aqueous phenol and the allergenic extract is recovered from he phenol phase.

The polyaldehyde and polyketone reagents which lie within the scope of this invention include dialdehydes and diketones as well as the higher aldehydes and ketones. Generally of the polyketones and polyaldehydes which may be used we prefer to use dialdehydes, e.g. those having from two to about 24 carbon atoms in the molecule. The dialdehyde may be aliphatic, cycloaliphatic, heterocyclic or aromatic, and may have either a straight or branched chain structure, e. g. glyoxal, 1,3- propanedial, 1,4-butanedial, glutaraldehyde and a, ctr-dialdehydes having from 14 to 24 carbon atoms in the molecule. A particularly preferred dialdehyde is glutaraldehyde.

The term carbodiimide as used in the present specification refers to compounds of Formula I and salts thereof:

wherein R and R are the same or different and each is an aliphatio, aromatic or heterocyclic radical. The preferred carbodiimides for use in the present invention are water-soluble, e. g. l-cyclohexyl-3-( 2- morpholinoethyl) carbodiimide metho-p-toluenesulphonate.

As used herein the term epihalohydrin refers to compounds of Formula II:

Cfiz CHzCH2X (II) wherein X is a halogen atom, particularly bromine or chlorine. We find that good results are obtained with epichlorohydrin.

As examples of inorganic cyanate ion reagents may be mentioned the alkali metal cyanates, particularly potassium cyanate; and the alkaline earth metal cyanates.

As a general rule, allergenic proteins are fairly resistant to denaturation and can usually be heated to relatively high temperatures without denaturation taking place. The process of this invention can thus take place over a wide range of temperatures although in practice it will generally not be necessary or desirable to exceed a temperature of about C. When dialdehydes are employed it is preferred to operate at a temperature below 37C, and in practice we prefer to carry out the reaction at room temperature in each case, i.e. about 20 25C. When employing dialdehydes, extreme reaction conditions should be avoided in order to reduce undesirable byproducts such as are produced by self condensation of the aldehydes.

In the case of polyaldehydes and polyketones, the pH which the process of this invention should be carried out is not critical. A suitable pH range from about 4 to about 8, with a pH of about 5 being preferred. Very low pH values should be avoided in order to reduce possible self condensation of the aldehydes.

Similarly in the case of epihalohydrin and carbodiimides, the reaction can be carried out at any convenient pI-I, although we prefer to avoid extremes of pH. For the epihalohydrin the reaction proceeds smoothly at alkaline pI-Is, suitably at about pH 8. In the case of the carbodiimide, the reaction is preferably carried out at acid pHs, suitably at pH about 5.

The reaction of the allergenic protein with an inorganic cyanate reagent in the process of this invention must be carried out at acid pl-ls preferably at a pH of about 5.

The reagents used in the process of this invention are believed to act as cross-linking agents for the allergenic material, forming interand/or intra-molecular links. Thus, although the allergenic starting materials are water-soluble, the modified allergenic products of the present invention are usually only sparingly soluble. The solubility of the modified allergenic materials appears to be dependent on the extent of cross-linking, which in turn may vary according to such factors as the nature and quantityof reagent used and the reaction conditions. We are not aware of any empirical method of determining in advance the solubility characteristics of the modified allergenic products and consequently the reaction variables necessary to obtain a product having the desired solubility must be determined by trail and error. This is a matter of routine, however, and should present little difiiculty to those skilled in the art.

In another embodiment of this invention there is provided a pharmaceutical preparation comprising the modified allergenic material prepared by the process described above, and a parenterally acceptable carrier. Suitable carriers include isotonic salt or buffer solutions, oily carriers and other materials well known in the art. If desired an adjuvant such as tyrosine alumina, aluminum hydroxide or aluminum phosphate, may be included.

The modified allergenic material is generally admin istered by subcutaneous injection. Dosage rates will vary according to the allergic condition of the patient.

Generally, in preparing pharmaceutical compositions in accordance with this invention, the modified allergenic material should be one which has a reduced solubility relative to the starting material, but which is sufficiently soluble in vivo to provide the desired release characteristics. We find that one way of achieving this is to use a sparingly soluble modified allergen absorbed on alumina and like materials. The degree of solubility of the cross-linked allergenic material is modified by absorption onto the alumina and the optimum in vivo release characteristics can be achieved by routine experimentation.

On parenteral administration to animals of the modified allergenic materials of this invention, it has been found that appreciable levels of circulating antibody are formed, the antibody having cross-specificity for the unmodified allergenic material. The modified materials tested did not cause any anaphylactic reaction in hypersensitive animals.

EXAMPLE 1 Preparation of Insoluble Allergen Derivative with Glutaraldehyde A partially purified extract of Cocksfoot pollen, containing 10 mg. protein/ml in 0.1M sodium acetate buffer pH 5.3 (5 ml.), was treated with 0.5 percent glutaraldehyde solution (5 ml.), and stirred at room temperature for 30 minutes. The precipitate which formed was removed by centrifugation and washed with distilled water to remove residual soluble material. it was finally suspended in phenol-saline solution for storage. Test of Allergenicity The suspension of insolubilised pollen at a concentration of mg/ml. was pricked into. the skin of grasssensitive allergic patients. At the same time the starting material and phenol-saline solution respectively were pricked into other areas of skin of the same patients. Wheal areas were measured after 10 minutes, and are expressed in Table l in sq. mm. It can be seen that insolubilised material at 200 times the concentration of starting material has barely one tenth of its allergenicity: the retained allergenicity is thus negligible when compared with that of the starting material. Test of lmmunogenicity The insolubilized material and the starting material respectively were emulsified in Freunds complete adjuvant to give concentrations of 1 mg/ml. Groups of guinea-pigs were injected subcutaneously with one or other of the emulsions (0.5 ml.). After 22 days the animals were clipped free of hair on the flanks and a series of intradermal injections (0.1 ml.) of a serial dilution of purified Cocksfoot pollen extract was made into the clipped areas. A 5 percent solution of Pontarnine Sky Blue (0.4 ml.) was immediately injected intravenously. After 20 minutes wheal diameters were measured, and are recorded in Table 2.

It can be seen that not only does the glutaraldehydetreated material produce antibody which reacts with the starting material, but it is a more efficient immunizer than the starting material.

TABLE 1 Patient No. lnsolubilized Phenol- Purified Cocksfoot cocksfoot Saline pollen extract extract l0 mg/ml. 50 ,ug/ml 1 21 84 i2 2 16 32 9 3 13 57 23 4 I5 51 4 Total 65 224 48 Total less that for phenolsaline 1? 176 TABLE II Guinea lmmuni- Wheal diameter (mm.) for quantity of Cocksfoot pollen extract injected intradermally Pig sing Number material (0.5 mg) lOOug long Lug O.l,u.g 0.0l,u.g 0.00lug l Purified l5 0 0 0 0 0 cocksfoot 2 Pollen l6 0 0 O 0 0 Extract l7 0 0 0 0 O 4 l6 0 0 0 0 O 5 Glutaral4 0 0 0 0 0 ldehyde- 6 treated l2 l0 9 0 0 O cocksfoot 7 Pollen 14 1312 l2 l0 8 Extract 8 l6 l4 12 ll 10 8 9 l2 l0 0 0 0 0 l0 l2 9 O 0 0 0 EXAMPLE 2 Preparation of Carbodiimide-Treated Allergen Fifty mg of material which had been extracted from mixed grass pollens, and which had been partially purified by treatment with aqueous phenol and subsequent precipitation of protein from the phenol phase, so as to remove much of the carbohydrate and low molecular weight material, was dissolved in 5 ml. of 0.5 M. borate Table III:

TABLE III Patient Mixed grass Carbodiimide- Phenol No. pollen extract treated mixed saline 50 pig/ml grass pollen extract 6 62 3 0 Total 112 5 0 Figures indicate wheal areas (sq.mm.). Test of lmmunogenicity Replicate guinea pigs were immunized by subcutaneous injection of an emulsion containing the test material in Freunds complete adjuvant. A similar set of guinea pigs were immunized with the unmodified starting material adjuvanted in the same way. After 21-8 days the animals were clipped free of hair on the flanks and a series of intradermal injections (0.1 ml.) of a se' rial dilution of starting material terminating with normal saline was made into the clipped area.

A 5 percent solution of Pontamine Sky Blue (0.4 ml) was immediately injected intravenously. After 20 minutes blue-colored wheals formed at some of the sites of intradermal injection, indicating the presence of antibody with specificity for the starting material. Wheal diameters were measured and recorded.

The results of the immunogenicity tests are recorded in Table IV:

TABLE IV Guinea lmmunizing "-7, Wheat diameter (MMs) for Pig. No. Material quantity of mixed grass 5 pollen extract injected intradermally l g us 1 s as as pg 1 mixed [4 l2 l0 9 8 8 2 grass poll4 l3 l0 9 8 3 len exl6 14 12 1O 9 9 4 tract 14 13 lo 5 carbodiimide- 14 12 10 10 9 6 treated mixed 12 1O 7 grass pollen 12 10 9 9 9 8 extract It can be seen from the results shown in Tables Ill and IV that higher levels of antibody were produced by immunization with the carbodiimide modified allergen, but that the allergenicity of the material was negligible.

EXAMPLE 3 50 mg of material which had been extracted from mixed grass pollens, and which had been partially purified so as to remove much of the carbohydrate and low molecular weight material, was dissolved in 5 ml of 0.01 M phosphate buffer pH 8.0. 1 ml of 1-chloro-2; 3-epoxypropane was added slowly and the mixture was stirred overnight at room temperature. The precipitate which formed was centrifuged off, washed with phosphate buffer, and suspended in phenol saline.

Test of Allergenicity A Wheal of the test material and a solution of the starting material, both in phenol-saline, and the medium itself, were respectively pricked into the skin of grass sensitive allergic patients. Weal areas were measured after 10 minutes. The results of the test of allergenicity are shown in Table V:

Figures indicate wheal areas (sq.mm.). Test of lmmunogenicity Replicate guinea pigs were immunized by subcutaneous injection of an emulsion containing the test material in Freunds complete adjuvant. A similar set of guinea pigs were immunized with the unmodified starting material adjuvanted in the same way. After 21-8 days the animals were clipped free of hair on the flanks and a series of intradermal injections (0.1 ml) of a serial dilution of starting material terminating with normal saline was made into the clipped area.

A 5 percent solution of Pontamine Blue Sky (0.4 ml) was immediately injected intravenously. After 20 minutes blue-colored wheals formed at some of the sites of intradermal injection, indicating the presence of antibody with specificity for the starting material. Wheal diameters were measured and recorded. The results of the test of immunogenicity are shown in Table VI:

8 pollen exl tract mg) 9 mixed grass 12 9 l0 pollen exl4 l2 9 ll tract 12 l l 9 12 (0.5 mg) l4 l2 9 l3 Epichlorhyl0 8 l 4 drin-treated l5 grass pollen l0 8 l6 extract It can be seen from the above results that detectable levels of antibody were produced by immunization with epichlorhydrin-treated allergens while the allergenicity was reduced to a negligible level.

EXAMPLE 4 50 mg of material which had been extracted from Cocksfoot grass pollen was dissolved in 10 ml of 0.01 M pH 8.0. 1 ml of lbromo-2:3-epoxy propane was added slowly and the mixture was stirred overnight at room temperature. The precipitate which formed was centrifuged off, washed with phosphate buffer, and suspended in phenol saline.

Results of the biological testing are shown in Tables III and IV. The testing procedures were identical with those of Example 3. Detectable levels of antibody were produced by immunization, while allergenicity was reduced to negligible levels.

TABLE VI] lmmunogenicity of Epibromehydrin-Treated Allergen Allergenicity of Epibromohydrin-Treated Allergen Patient Cocksfoot Epibromohydrintreated Cocksfoot pollen extract l00 #g/ml Phenol extract No. l00 Lg/ml saline 1 9 0 0 2 l8 0 0 3 22 O 0 4 2i 0 0 Total 70 0 0 EXAMPLE 5 Preparation of Cyanate Modified Allergen An aqueous extract of mixed grass pollens (Bent, Broom, Cocksfoot, Dogstail, False Oat, Fescue, Foxtail, Meadow Rye, Timothy Vernal and Yorkshire Fog) was partially purified by treatment with aqueous phenol followed by precipitation of protein from the phenol phase to remove much of the carbohydrate and the low molecular weight materials. 50 mg of the resultant partially purified allergenic protein was dissolved in 5 ml of water and the pH adjusted to pH 8 by the addition of sodium hydroxide solution. The pH was then further adjusted 5.0 with acetic acid, 0.2 g of potassium cyanate was added, and the mixture stirred at room temperature overnight. The precipitate which formed was washed repeatedly with phosphate buffer at pH 8 and then suspended in phenol saline. Test of Allergenicity A suspension of the cyanate-modified allergen prepared as above, a suspension of the unmodified partially purified allergen extract (both in phenol saline) and the phenol-saline medium itself were respectively pricked into the skin of grass-sensitive allergic patients. Wheal areas were measured after 10 minutes and are expressed in Table IX in sq. mm. It can be seen that the cyanate modified allergen exhibits negligible allergenicity relative to the unmodified material.

Total Test of Immunogenicity Replicate guinea pigs were immunized by subcutaneous injection of an emulsion containing the cyanatemodified allergen in Freunds complete adjuvant. A similar set of guinea pigs were immunized with the unmodified starting material adjuvanted in the same way. After 21-28 days both sets of animals were clipped free of hair on the flanks and a series of intradermal injections (0.1 ml) of a serial solution of the starting material terminating with normal saline was made into the clipped area.

A 5 percent solution of Pontamine skyblue (0.4 ml) was immediately injected intravenously. After 20 minutes blue-colored wheals formed and some of the sites of intradermal injection, indicating the presence of antibody with specificity for the starting material. Again wheal diameters were measured and are recorded in Table X. It can be seen that the cyanate modified allergen retains the immunizing specificity of the starting material.

TABLE X wheal diameter (mms) for quantity of mixed grass pollen extract injected i.d.

9 Mixed grass l4 l2 9 l pollen extract 12 l l 9 l l (0.5 mg) 14 12 9 l2 l2 9 EXAMPLE 6 In order to obtain confirmation of the biological testing results the procedure of Example was repeated. The results of the test of the allergenicity of the modified allergen are recorded in Table XI and the results of the tests of the immunogenicity of the cyanatemodified allergen are recorded in Table XII.

TABLE XI Mixed grass Cyanate-treated Patient pollen extract mixed grass Phenol No. 100 #g/ml pollen extract saline 2 mg/ml l 23 l 1 2 6 0 0 3 2 0 0 4 l9 0 0 Total 50 l l Figures indicate Wheal areas (sq.mm.).

TABLE XII Whealdiameter (mms) for quantity of mixed grass pollen extract injected i.d.

Guinea lmmunizing Pig No. material 0.l 0.0

l00y.g lOpg lug g p.g 0.00lp.g

1 Mixed grass l2 l0 9 8 2 pollen extract l2 l0 7 3 (5 mg) l2 l0 8 4 l2 l0 9 5 Cyanate-treated l2 l0 6 mixed grass 12 9 7 pollen extract l4 l2 9 8 (5 mg) 14 10 9 Mixed grass l4 l0 l0 pollen extract 12 l l 9 11 (0.5 mg) 10 9 l2 l3 Cyanate-treated l2 1 l 8 14 mixed grass 12 l5 pollen extract 10 l6 (0.5 mg) EXAMPLE 7 Treatment of Pollen Extract with Phenyl Glyoxal Method A 3 percent solution of phenylglyoxal hydrate dissolved in 0.01 M phosphate buffer, pH 8 was added to an equal volume of 50 mg of material which had been extracted from cocksfoot pollen and which, after purification by treatment with phenol, was dissolved in the same buffer. The reaction was carried out at room temperature for 24 hours. The precipitate which formed was washed repeatedly with phosphate buffer at pH 8 and then suspended in phenol saline. Test of Allergenicity A suspension of the phenylglyoxaI-modified material prepared as above, a suspension of the unmodified phenol treated Cocksfoot extract (both in phenol-saline) and the phenol-saline medium itself were respectively pricked into the skin of grass-sensitive allergic patients.

Wheal areas were measured after 10 minutes and are expressed in Table XIII in sq. mm.

Test of Immunogenieity Replicate guinea pigs were immunized by subcutaneous injection of an emulsion containing the phenylglyoxal modified material in Freunds complete adjuvant. A similar set of guinea pigs were immunized with the unmodified starting material adjuvanted in the same way. After 28 days, both sets of animals were clipped free of hair on the flanks and a series of intradermal injections (0.1 ml) of a serial solution of the starting material terminating with normal saline was made into the clipped area. A 5 percent solution of Pontamine sky blue (0.4 ml) was immediately injected intravenously. After 20 minutes blue colored wheals formed at some of the sites of intradermal injection, indicating the presence of antibody with specificity for the starting material. Wheal areas were measured and are recorded in Table XIV.

TABLE XIV Wheal diameter (mm) for quantity of Cocksfoot pollen extract injected i.d.

Treatment of Pollen Extract with Glutaraldehyde and Subsequent Absorption into Aluminum Hydroxide Method 1 ml of 5 percent glutaraldehyde solution was added to 9 ml of an aqueous extract of timothy pollen containing 1 mg/ml at pH 5.3. The mixture was stirred at room temperature for 3 days. 6 ml of 2 percent aluminium hydroxide solution were added and the mixture stirred for 1 hour. After centrifugation the precipitate was washed twice in 0.01 M phosphate bufier pH 8 and three times in distilled water and finally resuspended to a concentration of 1 mg/ml pollen in phenol saline. The procedure was repeated without the addition of glutaraldehyde, the final suspension serving as a control in the immunizing specificity test. Test of Allergenicity A suspension of the above material, a solution of the unmodified pollen extract (both in phenol-saline) and the phenol saline medium itself were respectively pricked into the skin of grass-sensitive allergic patients. Wheal areas were measured after 10 minutes and are expressed in Table XV in sq. mm.

Test of immunizing Specificity Replicate guinea pigs were immunized by subcutaneous injection of the alumina-glutaraldehyde adsorbed modified material. A similar set of guinea pigs were immunized with unmodified alumina-adsorbed. timothy pollen extract at a pollen concentration of 1 mg/ml. 21 days later a repeat injection was given and the animals bled 10 days later.

Passive cutaneous anaphylaxis was carried out on the sera by injection of serial dilutions intradermally into a clipped area on the flanks of a set of guinea pigs. The pigs were then challenged intravenously with the un- -modified aqueous timothy extract, containing 0.4 ml Pontamine sky blue solution, 5 hours later. Results obtained with difierent concentrations of challenging antigen areshown in Table XVl for the modified material and Table XVII for the control suspension without glutaraldehyde.

Challenge freeze- Wheal diameters in dried aqueous at serum dilution Guinea timothy pollen pig No. extract 1/5 1/25 1/125 1/625 1/3125 Selim 1 1 rngJml 22 20 100 ngJm 20 17 rig/ml 18 5 lg/ml--- 14 TABLE XVII Challenge ireeze- Wheel diameters in mm. at serum dilution dnecl aqueous of- Guinea timothy pollen pig No. extract 1/5 1/25 1/125 1/625 1/3125 Saline We claim:

1. A parenterally administrable anti-allergenic pharmaceutical preparation comprising a modified allergenic material in an amount sufficient to combat allergies and a pharmaceutically acceptable carrier, said modified allergenic material being an allergenic protein or glycoprotein which is crosslinked intcror intramolecularly with a dialdehyde of two to 24 carbon atoms, a carbodiimide, an epihalohydrin or an inorganic cyanate, said modified allergenic material being substantially water-insoluble or only sparingly water-soluble and having a reduced allergenicity relative to the uncrosslinked allergenic protein or glycoprotein and having the ability to produce antibodies having crossspecificity for the uncrosslinked allergenic protein or glycoprotein.

2. A pharmaceutical preparation according to claim 1 further comprising an adjuvant.

3. A pharmaceutical preparation according to claim 2 wherein the adjuvant is selected from tyrosine, alumina, aluminum hydroxide and aluminum phosphate.

4. A pharmaceutical preparation according to claim 3 wherein the adjuvant is tyrosine.

5. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is crosslinked to said dialdehyde.

6. A pharmaceutical composition according to claim 5 wherein the dialdehyde is an cue-dialdehyde of 14 to 24 carbon atoms.

7. A pharmaceutical preparation according to claim 5 wherein the dialdehyde is 1,3-propanedial, 1,4- butanedial, glutaraldehyde or phenyl glyoxal hydrate.

8. A pharmaceutical preparation according to claim 1 wherein said modified allergenic material is cross- 9. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said carbodiimide.

10. A pharmaceutical preparation according to claim 9 wherein the carbodiimide is l-cyclo-hexyl-3-(2- morpholinoethyl) carbodiimide metho-p-toluenesulphonate.

11. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said epihalohydrin.

12. A pharmaceutical preparation according to claim 11 wherein the epihalohydrin is epichlorohydrin.

13. A pharmaceutical preparation according to claim 11 wherein the epihalohydrin is l-bromo-2,3- epoxypropane.

14. A pharmaceutical composition according toclaim 1 wherein said modified allergenic material is cross-linked to said inorganic cyanate.

15. A pharmaceutical preparation according to claim 11 wherein said inorganic cyanate is an alkali metal cyanate or an alkaline earth metal cyanate.

16. A pharmaceutical preparation according to claim- 11 wherein said inorganic cyanate is potassium cyanate. 

2. A pharmaceutical preparation according to claim 1 further comprising an adjuvant.
 3. A pharmaceutical preparation according to claim 2 wherein the adjuvant is selected from tyrosine, alumina, aluminum hydroxide and aluminum phosphate.
 4. A pharmaceutical preparation according to claim 3 wherein the adjuvant is tyrosine.
 5. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said dialdehyde.
 6. A pharmaceutical composition according to claim 5 wherein the dialdehyde is an Alpha , omega -dialdehyde of 14 to 24 carbon atoms.
 7. A pharmaceutical preparation according to claim 5 wherein the dialdehyde is 1,3-propanedial, 1,4-butanedial, glutaraldehyde or phenyl glyoxal hydrate.
 8. A pharmaceutical preparation according to claim 1 wherein said modified allergenic material is cross-linked to glutaraldehyde.
 9. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said carbodiimide.
 10. A pharmaceutical preparation according to claim 9 wherein the carbodiimide is 1-cyclo-hexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene-sulphonate.
 11. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said epihalohydrin.
 12. A pharmaceutical preparation according to claim 11 wherein the epihalohydrin is epichlorohydrin.
 13. A pharmaceutical preparation according to claim 13 wherein the epihalohydrin is 1-bromo-2,3-epoxypropane.
 14. A pharmaceutical composition according to claim 1 wherein said modified allergenic material is cross-linked to said inorganic cyanate.
 15. A pharmaceutical preparation according to claim 14 wherein said inorganic cyanate is an alkali metal cyanate or an alkaline earth metal cyanate.
 16. A pharmaceutical preparation according to claim 15 wherein said inorganIc cyanate is potassium cyanate. 